Tziveleka Leto-Aikaterini, Kontoyianni Christina, Sideratou Zili, Tsiourvas Dimitris, Paleos Constantinos M
Institute of Physical Chemistry, NCSR "Demokritos", 15310 Aghia Paraskevi, Attiki, Greece.
Macromol Biosci. 2006 Feb 10;6(2):161-9. doi: 10.1002/mabi.200500181.
Multifunctional hyperbranched polyether polyols bearing protective poly(ethylene glycol) (PEG) chains with or without the folate targeting ligand at their end have been prepared. Solubilization in these polymers of a fluorescent probe, pyrene, and an anticancer drug, tamoxifen, was physicochemically investigated. It was found that PEG chains attached at the surface of these hyperbranched polymers, in addition to their well-established protective role, enhance the encapsulation efficiency of the polymers. The release of pyrene and tamoxifen observed upon addition of sodium chloride is, in most of the cases, significant only at concentrations exceeding the physiological extracellular concentration. Thus, a significant amount of the probe or drug remains solubilized inside the carriers, which is an encouraging result if the polymers are to be used for drug delivery.
已制备出末端带有或不带有叶酸靶向配体的、带有保护性聚乙二醇(PEG)链的多功能超支化聚醚多元醇。对荧光探针芘和抗癌药物他莫昔芬在这些聚合物中的增溶作用进行了物理化学研究。结果发现,连接在这些超支化聚合物表面的PEG链,除了其已确立的保护作用外,还提高了聚合物的包封效率。在大多数情况下,加入氯化钠后观察到的芘和他莫昔芬的释放,仅在浓度超过生理细胞外浓度时才显著。因此,大量的探针或药物仍溶解在载体内部,如果将这些聚合物用于药物递送,这是一个令人鼓舞的结果。